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279 results for “Mediterranean Region”
Fig. 5 in Revision of the Genus Schizoretepora (Bryozoa, Cheilostomatida) from the Atlantic-Mediterranean region
Fig. 5. Schizoretepora solanderia (Risso, 1826), Menorca Channel (A–B, D, G–H: MZB 2014-1471; C, E–F: MZB 2014-1486). A. Colony view. B. Detail of aperture. C. Growing margin with autozooids showing up to six spines. D. Older ovicellate autozooids with giant vicarious avicularia. E. Detail of articulated and carenated spines. F. Marginal avicularia showing nested piling of cystids. G. Details of ovicell. H. Abfrontal view with avicularia.
Fig. 11 in Revision of the Genus Schizoretepora (Bryozoa, Cheilostomatida) from the Atlantic-Mediterranean region
Fig. 11. Schizoretepora sp. nov. (= S. imperati sensu O'Donoghue & de Watteville 1939), from Schizoretepora imperati, coll. O'Donoghue (NHMUK 1963.9.4.12). A. Colony view. B. Primary orifice showing distal denticles and proximal condyles. C. Autozooids with giant avicularia. D. Large vicarious avicularia on cystid. E. Abfrontal view. F. Detail of abfrontal avicularium and rugose surface.
Fig. 3 in Revision of the Genus Schizoretepora (Bryozoa, Cheilostomatida) from the Atlantic-Mediterranean region
Fig. 3. Principal component analysis (PCA) biplot based on metric characters of the species Schizoretepora aviculifera (Canu & Bassler, 1930), S. granulosa (Canu & Bassler, 1930), S. hassi Harmelin, Bitar & Zibrowius, 2007, S. imperati (Busk, 1884), S. imperati sensu O'Donoghue & de Watteville 1939, S. imperati of other authors, S. longisetae (Canu & Bassler, 1928) and S. pungens (Canu & Bassler, 1925).
Fig. 10 in Revision of the Genus Schizoretepora (Bryozoa, Cheilostomatida) from the Atlantic-Mediterranean region
Fig. 10. Schizoretepora pungens (Canu & Bassler, 1925). A from Schizoretepora imperati, coll. Gautier (MNHN-IB-2008-11299); B, F from Schizoretepora pungens (MNHN-IB-2008-14434); C from Schizoretepora pungens, holotype, coll. Canu (MNHN-IB-2014-20); D from specimen labelled as Schizoretepora imperati (MNHN-IB-2008-9955); E, G from specimen labelled as Schizoretepora longisetae, coll. Canu (MNHN-IB-2014-19); H from Schizoretepora pungens (MNHN-IB-2008-14045). A–B. Two ovicell aspects in young colonies. C. Deeply immersed ovicells in older colonies. D. Abfrontal face showing rugose kenozooids separated by raised sutures. E. Abfrontal face showing two types of adventitious avicularia, both oval and almond-shaped. F. Abfrontal detail of giant avicularium at the basis of a fenestra and small oval avicularia. G. Aspect of spinose colony. H. Aspect of serrated colony.
Fig. 4. Schizoretepora calveti d in Revision of the Genus Schizoretepora (Bryozoa, Cheilostomatida) from the Atlantic-Mediterranean region
Fig. 4. Schizoretepora calveti d'Hondt, 1975, lectotype (MNHN-IB-2008-7565). A. Colony view. B. Detail of aperture and avicularia. C. Young autozooids and avicularia in frontal view. D. Older autozooids and avicularia in frontal view. E. Ovicellate zooids. F. Abfrontal view with avicularia.
Fig. 2 in Revision of the Genus Schizoretepora (Bryozoa, Cheilostomatida) from the Atlantic-Mediterranean region
Fig. 2. Dendrogram on qualitative characters (frontal shield surface; frequency of frontal pores; peristome shape; frequency of adventitious avicularia, abfrontal vicarious avicularia, abfrontal oval adventitious avicularia and abfrontal triangular adventitious avicularia; abfrontal surface; ovicell shape) of the species that constitute the imperati-group: S. aviculifera (Canu & Bassler, 1930), S. granulosa (Canu & Bassler, 1930), S. imperati (Busk, 1884), S. imperati from other authors, S. longisetae (Canu & Bassler, 1928) and S. pungens (Canu & Bassler, 1925). Schizoretepora "imperati" sensu O'Donoghue & de Watteville 1939 has been excluded from the analysis because it lacks ovicells.
Fig. 9 in Revision of the Genus Schizoretepora (Bryozoa, Cheilostomatida) from the Atlantic-Mediterranean region
Fig. 9. Schizoretepora pungens (Canu & Bassler, 1925). A from specimen labelled as Schizellozoon longisetae, Gautier leg. (MNHN-IB-2008-11127); B, H from specimen labelled as Retepora imperati, coll. Canu (MNHN-IB-2014-29); C from specimen labelled as Schizellozoon longisetae (MNHN-IB-2008-14462); D from Schizoretepora pungens, holotype, coll. Canu (MNHN-IB-2014-20); E from Schizoretepora pungens (MNHN-IB-2008-14434); F from specimen labelled as Retepora imperati (MNHN-IB-2008-982); G from specimen labelled as Retepora imperati, coll Calvet (MNHN-IB-2008-6052). A. Young colony with spines. B. Primary orifice showing distal denticles, proximal condyles, sinus and smothered peristome. C. Young autozooids showing spines and acute peristomes. D. Old autozooids lacking spines and with smothered peristomes. E. Detailed view of articulated and carenated club-like spines. F. Adventitious triangular (upper side) and oval (bottom right) avicularians. G. Giant avicularium at basis of fenestra. H. Giant avicularia on large cystids showing crossbar without columella.
Fig. 1 in Revision of the Genus Schizoretepora (Bryozoa, Cheilostomatida) from the Atlantic-Mediterranean region
Fig. 1. Preparations of the 'imperati-group': Schizoretepora aviculifera (Canu & Bassler, 1930) (MNHN-IB-2014-24), S. granulosa (Canu & Bassler, 1930) (MNHN-IB-2014-21), S. imperati (Busk, 1884) (MNHN-IB-2014-29), S. longisetae (Canu & Bassler, 1928) (MNHN-IB-2014-19) and S. pungens (Canu & Bassler, 1925) (MNHN-IB-2014-20). Specimens located at the Departments of Zoology and Paleontology of the MNHN in Paris.
Figure 2 in Unusual wintering records of pipits (Aves: Motacillidae) in Hatay, Eastern Mediterranean Region of Turkey
Figure 2. The total number of observations in comparison with the number of records of each pipit species during the 4 months of the winter period in the study.
Figure 2 in A new form of Melitaea phoebe (Goeze, 1779) (Lepidoptera) from the Mediterranean region (Turkey)
Figure 2. Habitus and male genitalia of Melitaea phoebe, new form. a, b: Habitus; c, d: male genitalia.
Figure 3 in A new form of Melitaea phoebe (Goeze, 1779) (Lepidoptera) from the Mediterranean region (Turkey)
Figure 3. Habitus and male genitalia of Melitaea punica telona (=M. ornata). a, b: Habitus; c, d: male genitalia.
Atmospheric moisture recycling in Mediterranean-type climate regions across the world
<p>Please cite the corresponding manuscript when using this data:</p> <p>... (information will follow as soon as the manuscript is published)</p> <p>This dataset includes the local precipitation recycling ratios and the regional moisture recycling ratios for five major Mediterranean-type climate regions across the globe. Below we list these five regions and explain the concepts of local precipitation recycling and regional moisture recycling. </p> <p> </p> <p><strong>Mediterranean-type climate regions</strong></p> <p>Region 1: South West Australia</p> <p>Region 2: West coast of the US (California)</p> <p>Region 3: Central Chile</p> <p>Region 4: Mediterranean Basin (region around the Mediterranean Sea)</p> <p>Region 5: The Cape region of South Africa</p> <p> </p> <p><strong>Local precipitation recycling ratio</strong></p> <p>The local precipitation recycling ratio is the fraction of precipitation that originated within approximately 50 km from where it rains out, i.e., it evaporated from the grid cell where it rains out and the 8 surrounding grid cells. The grid cells have a resolution of 0.5DEGx0.5DEG. A more detailed explanation is provided in the journal article Theeuwen et al. (2024). </p> <p>The files that include local precipitation recycling ratios are:</p> <table> <tbody> <tr> <td><strong>File name</strong></td> <td><strong>Study region</strong></td> <td><strong>Time dimension (month)</strong></td> <td><strong>Latitude range</strong></td> <td><strong>Longitude range</strong></td> </tr> <tr> <td>PLMR_SWAustralia.nc</td> <td>South West Australia</td> <td>January-December</td> <td>-15:-48 DEGN</td> <td>106:154 DEGE</td> </tr> <tr> <td>PLMR_California.nc</td> <td>West coast of the US (California)</td> <td>January-December</td> <td>52:20 DEGN</td> <td>-131:-105 DEGE</td> </tr> <tr> <td>PLMR_CentralChile.nc</td> <td>Centra Chile</td> <td>January-December</td> <td>-10:-54 DEGN</td> <td>-80:-60 DEGE</td> </tr> <tr> <td>PLMR_Med_Basin.nc</td> <td>Mediterranean Basin</td> <td>January-December</td> <td>48:23 DEGN</td> <td>-20:-45 DEGE</td> </tr> <tr> <td>PLMR_SWCapeSA.nc</td> <td>The Cape region of South Africa</td> <td>January-December</td> <td>-26:-40 DEGN</td> <td>10:38 DEGE</td> </tr> </tbody> </table> <p> </p> <p><strong>Regional moisture recycling ratio</strong></p> <p>The regional moisture recycling ratio data includes both regional evaporation recycling ratios as well as regional precipitation recycling ratios. </p> <p>The regional evaporation recycling ratio is the fraction of evaporated water that rains out within the Mediterranean region it evaporated from. </p> <p>The regional precipitation recycling ratio is the fraction of precipitation that originated from the Mediterranean region it rains out in. </p> <p>This data has a resolution of 0.5DEGx0.5DEG and is a multi-year average (years: 2008-2017). A more detailed description is provided in the journal article Theeuwen et al. (2024). </p> <table> <tbody> <tr> <td><strong>Filename</strong></td> <td><strong>Type of recycling</strong></td> <td><strong>Study region</strong></td> </tr> <tr> <td>ERMR_SWAustralia.nc</td> <td>Regional evaporation recycling</td> <td>South West Australia </td> </tr> <tr> <td>ERMR_California.nc</td> <td>Regional evaporation recycling</td> <td>West coast of the US (California)</td> </tr> <tr> <td>ERMR_CentralChile.nc</td> <td>Regional evaporation recycling</td> <td>Centra Chile</td> </tr> <tr> <td>ERMR_Med-Basin.nc</td> <td>Regional evaporation recycling</td> <td>Mediterranean Basin</td> </tr> <tr> <td>ERMR_CapeSA.nc</td> <td>Regional evaporation recycling</td> <td>The Cape region of South Africa</td> </tr> <tr> <td>PRMR_SWAustralia.nc</td> <td>Regional precipitation recycling</td> <td>South West Australia </td> </tr> <tr> <td>PRMR_California.nc</td> <td>Regional precipitation recycling</td> <td>West coast of the US (California)</td> </tr> <tr> <td>PRMR_CentralChile.nc</td> <td>Regional precipitation recycling</td> <td>Centra Chile</td> </tr> <tr> <td>PRMR_Med-Basin.nc</td> <td>Regional precipitation recycling</td> <td>Mediterranean Basin</td> </tr> <tr> <td>PRMR_CapeSA.nc</td> <td>Regional precipitation recycling</td> <td>The Cape region of South Africa</td> </tr> </tbody> </table>
Linked collectors and determiners for: Review of the genus Trichactia Stein (Diptera: Tachinidae) in the Palaearctic Region, with the description of a new species from Iran and the East Mediterranean.
Natural history specimen data linked to collectors and determiners held within, "Review of the genus Trichactia Stein (Diptera: Tachinidae) in the Palaearctic Region, with the description of a new species from Iran and the East Mediterranean". Claims or attributions were made on Bionomia by volunteer Scribes, <a href="https://bionomia.net/dataset/dfb42b32-32b8-4e81-9caa-702a249d7845">https://bionomia.net/dataset/dfb42b32-32b8-4e81-9caa-702a249d7845</a> using specimen data from the dataset aggregated by the Global Biodiversity Information Facility, <a href="https://gbif.org/dataset/dfb42b32-32b8-4e81-9caa-702a249d7845">https://gbif.org/dataset/dfb42b32-32b8-4e81-9caa-702a249d7845</a>. Formatted as a Frictionless Data package.
Linked collectors and determiners for: On the genus Sunius Stephens, 1829 of Turkey. V. A new micropterous species from central southern Anatolia, with additional records from the western Mediterranean region (Coleoptera: Staphylinidae: Paederinae).
Natural history specimen data linked to collectors and determiners held within, "On the genus Sunius Stephens, 1829 of Turkey. V. A new micropterous species from central southern Anatolia, with additional records from the western Mediterranean region (Coleoptera: Staphylinidae: Paederinae)". Claims or attributions were made on Bionomia by volunteer Scribes, <a href="https://bionomia.net/dataset/ca210c1e-3b76-4b04-8576-57e86ae50caa">https://bionomia.net/dataset/ca210c1e-3b76-4b04-8576-57e86ae50caa</a> using specimen data from the dataset aggregated by the Global Biodiversity Information Facility, <a href="https://gbif.org/dataset/ca210c1e-3b76-4b04-8576-57e86ae50caa">https://gbif.org/dataset/ca210c1e-3b76-4b04-8576-57e86ae50caa</a>. Formatted as a Frictionless Data package.
Figure 6 in Species of genus Schizotheca Hincks (Bryozoa, Cheilostomata) described in the Atlantic-Mediterranean region, with notes on some species of Parasmittina Osburn
Figure 6. Schizotheca aviculifera. (A) Group of zooids (MNHN-14754); (B) view in perspective, showing the position of adventitious avicularia (MNHN-14748); (C) two ovicellate zooids, one of them with three spines (right) (MNHN-14748); (D) two orifices, showing poorly developed proximal teeth, and condyles with wavy distal edge (MNHN-14754); (E) orifice with well-developed proximal teeth (MNHN-14748); (F) a vicarious avicularium, showing Y-shaped foramen (MNHN-14754).
Figure 7 in Species of genus Schizotheca Hincks (Bryozoa, Cheilostomata) described in the Atlantic-Mediterranean region, with notes on some species of Parasmittina Osburn
Figure 7. Schizotheca aviculifera. (A–C) Casablanca, lectotype: (A) general view, showing orifices filled with sand; (B) orifice with well-developed proximal teeth; (C) orifice showing poorly developed proximal teeth. (D–F) Fedhala (as Schizotheca serratimargo): (D) general view, showing calcified zooids, and vicarious and adventitious avicularia; (E) orifice with well-developed proximal teeth; (F) orifice showing poorly developed proximal teeth.
Figure 5 in Species of genus Schizotheca Hincks (Bryozoa, Cheilostomata) described in the Atlantic-Mediterranean region, with notes on some species of Parasmittina Osburn
Figure 5. (A–C) Schizotheca buski sp. nov.: (A) group of ovicellate zooids with lanceolate adventitious avicularia (NHM-1899.7.1.5063, paratype); (B) a vicarious avicularium and a kenozooid with a porous plate (left) (NHM- 1899.7.1.5199, holotype); (C) primary orifice (NHM-1899.7.1.5199, holotype). (D–F) Schizotheca tuberigera: (D) group of autozooids, some ovicellate, with adventitious avicularia and a vicarious avicularium (MNHN-14121); (E) group of kenozooids with adventitious avicularia (MNHN-13831); (F) primary orifice (MNHN-14061).
Figure 3 in Species of genus Schizotheca Hincks (Bryozoa, Cheilostomata) described in the Atlantic-Mediterranean region, with notes on some species of Parasmittina Osburn
Figure 3. Schizotheca fissa. Ría de Ferrol, NW Iberian Peninsula. (A) General view of the colony; (B, C) two primary orifices; (D) ancestrula and early astogenesis; (E) detail of the ancestrula.
Figure 4 in Species of genus Schizotheca Hincks (Bryozoa, Cheilostomata) described in the Atlantic-Mediterranean region, with notes on some species of Parasmittina Osburn
Figure 4. (A–E) Schizotheca carmenae sp. nov.: (A) growing edge of the colony, showing adventitious avicularia (MNHN-7519); (B) growing edge of the colony, showing adventitious and vicarious avicularia (MNHN-7426, holotype); (C) primary orifice (MNHN-7426, holotype); (D) an ovicellate zooid with adventitious avicularia (MNHN-7426, holotype); (E) group of zooids at the growing edge, showing adventitious and vicarious avicularia (Sagres, Portugal, photograph: J.-G. Harmelin). (F, G) Schizotheca buski sp. nov.: (F) general view of the colony, showing two rows made of vicarious avicularia and kenozooids (NHM-1899.7.1.5199, holotype); (G) growing edge of the colony, showing vicarious avicularia (below) and oval adventitious avicularia (left above) (NHM- 1963.4.18.23).
Figure 1 in Species of genus Schizotheca Hincks (Bryozoa, Cheilostomata) described in the Atlantic-Mediterranean region, with notes on some species of Parasmittina Osburn
Figure 1. Parasmittina talismani. (A) View of the colony (MNHN-299, holotype); (B) view in perspective, showing the development of the peristome and adventitious avicularia (MNHN-299, holotype); (C) an ovicellate zooid (MNHN- 1037); (D) primary orifice and adventitious avicularia (MNHN-1037); (E) primary orifice and adventitious avicularium (MNHN-299, holotype); (F) two broken zooids showing the lyrula, the adventitious avicularia and the remaining basis of spines under the ovicells (MNHN-1037); (G) growing edge of the colony (MNHN-299, holotype).
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Allen Brain Atlas
Allen Brain Atlas is an Allen Institute collection of brain map atlases, datasets, APIs, and analysis tools covering mouse, human, and non-human primate brain resources.
Annotated Behaviour and Observability Dataset (ABODe)
ABODe is a University of Edinburgh DataShare dataset for behavior classification in group-housed mice using home-cage video, identities, bounding boxes, ground-plate positions, and annotator labels.
DANDI Archive for NWB datasets
DANDI is a BRAIN Initiative archive for publishing and sharing neurophysiology data, including electrophysiology, optophysiology, and behavioral data packaged as NWB and related standards.
International Brain Laboratory public data
The International Brain Laboratory public data releases expose standardized mouse decision-making experiments, including Neuropixels recordings, widefield calcium imaging, behavior, and session metadata accessed through the ONE API.
OpenNeuro
OpenNeuro is a free, open platform for sharing neuroimaging datasets, with public search, dataset pages, and download paths for web, S3, DataLad, and the OpenNeuro CLI.